Study register · detailKohortenstudie · Epilepsy · 2025
UK Medical Cannabis Registry: A Clinical Outcomes Analysis for Epilepsy.
Cowley et al.·Brain and behaviorImpact 2.2
Clear benefitGRADELow1 citations
Samplen = 134 Pat.
Duration6 months
EndpointQOLIE-31
Blindingn.a.
DesignKohortenstudie
”Key finding
Cannabis-based medicinal products were associated with improvements in all measured quality of life and health parameters (QOILE-31, sleep quality, EQ-5D-5L, anxiety, global impression); 29,85% of patients achieved clinically meaningful improvement.
Summary
UK Medical Cannabis Registry: Case series (n=134) on cannabis-based medicinal products (CBMPs) in treatment-resistant epilepsy. Improvements in QOLIE-31 and all HRQoL PROMs (p<0,050) at 1, 3 and 6 months vs. baseline; 40 patients (29,85%) achieved a clinically relevant difference in QOLIE-31 after 6 months. 18 adverse events (13,43%) in 5 patients (3,73%), predominantly mild/moderate.
P
PopulationAdults with treatment-resistant epilepsy from the UK Medical Cannabis Registry, n=134
I
InterventionCannabis-based medicinal products (CBMPs), type/dose not further specified
O
OutcomeSignificant improvements in QOLIE-31 and all HRQoL PROMs from baseline to 1, 3 and 6 months (p<0,050); 29,85% of patients achieved a clinically relevant difference in QOLIE-31 after 6 months; 18 AEs in 5 patients (3,73%), predominantly mild to moderate
Confidence in the evidence
Very lowLowModerateHigh
Low
The second of four GRADE levels, the effect estimate is of limited reliability.
Quality profile
Sample size★★★★★
Blinding—
Effect sizeClear benefit
Citations / year★★★★★
Authors
Cowley I, Erridge S, Aggarwal A, Evans L, Varadpande M, Clarke E, McLachlan K, Coomber R, Iqbal A, Rucker JJ
Background: A third of epilepsy patients fail to enter seizure remission despite optimal therapeutic management. Cannabis-based medicinal products (CBMPs) have shown promise as a potential therapy. However, a paucity of high-quality literature regarding CBMPs' efficacy and safety profile means further investigation is needed. The study aimed to examine changes in epilepsy-specific and general health-related quality of life (HRQoL) patient-reported outcome measures (PROMs) in individuals with treatment-resistant epilepsy.
Methods: A case series of patients with epilepsy from the UK Medical Cannabis Registry analyzed changes in Quality of Life in Epilpesy-31 (QOILE-31), Single-Item Sleep Quality Score (SQS), EQ-5D-5L, Generalized Anxiety Disorder-7 (GAD-7) and Patient Global Impression of Change (PGIC) between baseline, one, three, and six months. Adverse events (AEs) were collected and classified by severity. p < 0.050 was considered statistically significant.
Results: There were 134 patients included. Improvements were recorded from baseline to one, three, and six months in QOILE-31 and all HRQoL PROMs (p < 0.050). Forty patients (29.85%) reported a minimal clinically important difference in Quality of Life in Epilepsy-31 (QOLIE-31) at six months. There were 18 (13.43%) AEs reported by 5 (3.73%) patients, mainly mild and moderate.
Discussion: The proportion of patients achieving a clinically significant change is similar to existing CBMPs in epilepsy literature. AE incidence was lower than similar studies although this may be due to the large proportion (67.16%) of individuals who were not cannabis naive.
Conclusion: Initiation of CBMPs was associated with an improvement across all PROMs. CBMPs were well tolerated across the cohort. However, randomized controlled trials are needed to help determine causality.